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Effect of Oculomotor Therapy in Individuals With Convergence Insufficiency

U

University of Nove de Julho

Status

Not yet enrolling

Conditions

Convergence Insufficiency

Treatments

Other: Oculomotor therapy
Other: No Treatment Added

Study type

Interventional

Funder types

Other

Identifiers

NCT07036263
CI-2025

Details and patient eligibility

About

The aim of this study is to investigate the effect of oculomotor therapy in individuals with ocular convergence insufficiency.

Full description

Seventy participants with convergence insufficiency (CI) will be randomly allocated into two groups: Experimental Group (EG) (n=35) and Control Group (CG) (n=35). The primary outcome will be CI assessed by the convergence test. Secondary outcomes will include quality of life, postural balance, and gait speed. The EG will undergo five sessions of oculomotor therapy (once a week), based on and adapted from the established protocol for CI treatment. Results: Outcomes will be assessed by blinded evaluators at baseline, one week after the end of the treatment, and at 1 and 3 months follow-up. The CG will not receive any intervention. Data will be analyzed using statistical tests with a significance level set at p < 0.05.

Enrollment

70 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Individuals diagnosed with convergence insufficiency (CI);
  • Aged between 18 and 60 years;
  • Physically active individuals;
  • Without cognitive impairments;
  • Without vestibular system impairments (e.g., dizziness).

Exclusion criteria

  • Diagnosis of neurodegenerative diseases (e.g., Parkinson's, ALS);
  • Presence of dementia;
  • History of stroke;
  • Presence of vestibular disorders;
  • Systemic neuromuscular diseases;
  • Disabling musculoskeletal pain;
  • Diagnosis of diabetic polyneuropathy;
  • Use of joint prostheses;
  • Ongoing physical therapy treatment;
  • Lack of physical ability to perform the prescribed physical activities.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

70 participants in 2 patient groups

Experimental Group (EG)
Experimental group
Description:
This group will receive treatment with oculomotor therapy
Treatment:
Other: Oculomotor therapy
Control group (CG)
Other group
Description:
This group will not receive any type of treatment
Treatment:
Other: No Treatment Added

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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